Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10

MONDO:0014022

Any muscular dystrophy-dystroglycanopathy, type A in which the cause of the disease is a mutation in the RXYLT1 gene.

Also known as: RXYLT1 muscular dystrophy-dystroglycanopathy, type A, muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10, muscular dystrophy-dystroglycanopathy, type A caused by mutation in RXYLT1, MDDGA10, Walker-Warburg syndrome or muscle-eye-brain disease, Tmem5-related, muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 10

5 clinical trials for this condition and its sub-types, 0 tagged with Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 itself.

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↑ Muscular dystrophy-dystroglycanopathy, type A (1) ↑ Muscle-eye-brain disease (0)

Including sub-types (5) Tagged with Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 (0)

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